Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project-Reference-Cited by-同舟云学术

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Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project

Published:2009-12 Issue:12 Volume:11 Page:843-849
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Cotton Richard G.H.,Al Aqeel Aida I.,Al-Mulla Fahd,Carrera Paola,Claustres Mireille,Ekong Rosemary,Hyland Valentine J.,Macrae Finlay A.,Marafie Makia J.,Paalman Mark H.,Patrinos George P.,Qi Ming,Ramesar Rajkumar S.,Scott Rodney J.,Sijmons Rolf H.,Sobrido María-Jesús,Vihinen Mauno

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference17 articles.

Cited by 37 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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